Evidence map›Paper›PMID 40877177›Full record

ArticleIn vivo (Athens, Greece)

Multi-spin Redox Sensor for Electron Paramagnetic Resonance Studies of Tissue Redox State

Dessislava Lazarova, Biliana Nikolova, Zhivko Zhelev, Plamen Getsov, Milka Mileva, Rumiana Bakalova, Ichio Aoki

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Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Dessislava LazarovaFaculty of Medicine, Sofia University "St. Kliment Ohridski", Sofia, Bulgaria.
Biliana NikolovaInstitute of Biophysics and Biomedical Engineering, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Zhivko ZhelevInstitute of Biophysics and Biomedical Engineering, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Plamen GetsovFaculty of Medicine, Medical University, Sofia, Bulgaria.
Milka MilevaInstitute of Microbiology, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Rumiana BakalovaFaculty of Medicine, Sofia University "St. Kliment Ohridski", Sofia, Bulgaria; ra_bakalova@yahoo.com.
Ichio AokiInstitute for Quantum Medical Science, National Institutes for Quantum Science and Technology (QST), Chiba, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimRedox imaging is one of the fastest growing areas in diagnostics of pathologies accompanied by redox imbalance. We describe a multi-spin redox sensor (RS) and its application for redox imaging in mice using electron paramagnetic resonance (EPR) spectroscopy. MATERIALS AND

methodsThe probe is composed of a quantum dot functionalized with a cyclodextrin shell, conjugated with nitroxide residues (TEMPO) and triphenylphosphonium to achieve intracellular delivery. The data were validated with a conventional spin probe, mito-TEMPO. Nitroxide probe (RS or mito-TEMPO) was injected intravenously in mice under anesthesia. Blood samples were collected from the tail vein at four time intervals within 2 hours and subjected immediately to analysis using EPR spectroscopy. Two hours after injection, mice were sacrificed, five organs were isolated, and tissue homogenates were prepared and subjected to EPR analysis.

resultsRS had the same EPR contrast and significantly higher MRI contrast compared to mito-TEMPO. RS circulated longer in the bloodstream than mito-TEMPO, with both substances undergoing reduction in the blood. The distribution of RS and mito-TEMPO in different organs was equal, except for the brain. No adverse side effects were found in mice at the selected dose.

conclusionUsing a non-toxic nanoparticle in the chemical structure of RS as a carrier of nitroxide residues would enhance its translational relevance.

Indexed as

Spin LabelsAnimalsCyclic N-OxidesElectron Spin Resonance SpectroscopyMagnetic Resonance ImagingMiceNitrogen OxidesOxidation-ReductionQuantum DotsTissue DistributionCyclic N-OxidesNitrogen OxidesSpin LabelsTEMPOelectron paramagnetic resonance imagingmito-TEMPOredox sensorRedox state

Identifiers

PMID40877177
PMCPMC12396052

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.